List of variants in gene CUBN reported as not provided for anemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.7646C>T (p.Thr2549Met)	rs537292240	0.00009
NM_001081.4(CUBN):c.1000C>T (p.Gln334Ter)	rs561240556	0.00001
NM_001081.4(CUBN):c.1022A>G (p.Gln341Arg)	rs149517557	0.00001

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